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Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy

Duchenne muscular dystrophy, an X-linked disorder characterized by progressive muscle weakness, is the most common muscular dystrophy among children leading to death before the end of third decade. Anesthesia in such patients pose a great challenge due to various complications associated with it. Th...

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Autores principales: Kulshrestha, Ashish, Bajwa, Sukhminder Jit Singh, Singh, Amarjit, Kapoor, Vinod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173390/
https://www.ncbi.nlm.nih.gov/pubmed/25885395
http://dx.doi.org/10.4103/0259-1162.94788
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author Kulshrestha, Ashish
Bajwa, Sukhminder Jit Singh
Singh, Amarjit
Kapoor, Vinod
author_facet Kulshrestha, Ashish
Bajwa, Sukhminder Jit Singh
Singh, Amarjit
Kapoor, Vinod
author_sort Kulshrestha, Ashish
collection PubMed
description Duchenne muscular dystrophy, an X-linked disorder characterized by progressive muscle weakness, is the most common muscular dystrophy among children leading to death before the end of third decade. Anesthesia in such patients pose a great challenge due to various complications associated with it. The dreaded metabolic and clinical complications occur due to various inhalational anesthetics and succinylcholine in this subset of patients. We are reporting a child with diagnosed Duchenne muscular dystrophy who underwent excision of dentigerous cyst in oral cavity under procedural sedation with combination of dexmedetomidine and fentanyl and thus administration of general anesthesia was avoided.
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spelling pubmed-41733902014-10-22 Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy Kulshrestha, Ashish Bajwa, Sukhminder Jit Singh Singh, Amarjit Kapoor, Vinod Anesth Essays Res Case Report Duchenne muscular dystrophy, an X-linked disorder characterized by progressive muscle weakness, is the most common muscular dystrophy among children leading to death before the end of third decade. Anesthesia in such patients pose a great challenge due to various complications associated with it. The dreaded metabolic and clinical complications occur due to various inhalational anesthetics and succinylcholine in this subset of patients. We are reporting a child with diagnosed Duchenne muscular dystrophy who underwent excision of dentigerous cyst in oral cavity under procedural sedation with combination of dexmedetomidine and fentanyl and thus administration of general anesthesia was avoided. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC4173390/ /pubmed/25885395 http://dx.doi.org/10.4103/0259-1162.94788 Text en Copyright: © Anesthesia: Essays and Researches http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kulshrestha, Ashish
Bajwa, Sukhminder Jit Singh
Singh, Amarjit
Kapoor, Vinod
Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title_full Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title_fullStr Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title_full_unstemmed Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title_short Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy
title_sort dexmedetomidine and fentanyl combination for procedural sedation in a case of duchenne muscular dystrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173390/
https://www.ncbi.nlm.nih.gov/pubmed/25885395
http://dx.doi.org/10.4103/0259-1162.94788
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